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Article

No association of common VCP variants with sporadic frontotemporal dementia.

Neurobiology of aging - 1 Feb 2009

Schumacher Axel, Friedrich Patricia, Diehl Janine, Ibach Bernd, Schoepfer-Wendels Andreas, Mueller Jakob C, Konta Lidija, Laws Simon M, Kurz Alexander, Foerstl Hans, Riemenschneider Matthias

Abstract excerpt

Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD). To investigate the role of this novel gene in sporadic forms of frontotemporal dementia (FTD), we genotyped 27 single nuc...

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Source

Identifiers

PMID: 17618707
DOI: 10.1016/j.neurobiolaging.2007.05.023

Genes

VCP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17618707-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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No association of common VCP variants with sporadic frontotemporal dementia.PMID 17618707Read ↗

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Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.Semantic proximity Read ↗

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Three VCP Mutations in Patients with Frontotemporal Dementia.Semantic proximity Read ↗

Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.Semantic proximity Read ↗

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia.Semantic proximity Read ↗

Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene.Semantic proximity Read ↗

A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian FamilySemantic proximity Read ↗

VCP mutations in familial and sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

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